Jorge Alberto Hinojosa Camacho
FDA import alert and refusal historyPueblo Naolinco De Victoria, MexicoFEI 3011277091
As of October 26, 2026, Jorge Alberto Hinojosa Camacho (Pueblo Naolinco De Victoria, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for chayotes (choyote; chayote squash), published by FDA on January 10, 2018, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-05 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Jorge Alberto Hinojosa Camacho
1 record, newest first. Each line links to the FDA page it came from.
2018
- Import alert listingListed on Import Alert 99-05red listChayotes (Choyote; Chayote squash)Source
Questions about Jorge Alberto Hinojosa Camacho
- Is Jorge Alberto Hinojosa Camacho on an FDA import alert?
- Yes. As of October 26, 2026, Jorge Alberto Hinojosa Camacho is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for chayotes (choyote; chayote squash); FDA published the listing on January 10, 2018.
- Has FDA refused shipments from Jorge Alberto Hinojosa Camacho?
- No FDA import refusals for Jorge Alberto Hinojosa Camacho appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Jorge Alberto Hinojosa Camacho's FEI number?
- Jorge Alberto Hinojosa Camacho's FDA Establishment Identifier (FEI) is 3011277091.
- Can shipments from Jorge Alberto Hinojosa Camacho still enter the U.S.?
- Shipments of chayotes (choyote; chayote squash) from Jorge Alberto Hinojosa Camacho can be detained without physical examination under Import Alert 99-05; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.